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Smaïl Hadj-Rabia

Showing results (1-10 of 25) with videos related to

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Dermatology (Basel, Switzerland)|August 22, 2012
Tibial lymphoplasmacytic plaque: a new, illustrative case of a recently and poorly recognized benign lesion in childrenIsabelle Moulonguet, Smaïl Hadj-Rabia, Nicolas Gounod, et al.
Pediatric Dermatology|January 4, 2012
Congenital erosive and vesicular dermatosis: a new case and review of the literatureJacob Mashiah, Daniel Wallach, Stéphanie Leclerc-Mercier, et al.
European Journal of Human Genetics : EJHG|August 27, 2003
The Rapp-Hodgkin syndrome results from mutations of the TP63 geneGaëlle Bougeard, Smaïl Hadj-Rabia, Laurence Faivre, et al.
International Journal of Molecular Sciences|July 9, 2022
The Fate of Epidermal Tight Junctions in the <i>stratum corneum</i>: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin ConditionsMarek Haftek, Vinzenz Oji, Laurence Feldmeyer, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|April 8, 2014
Dento-maxillo-facial phenotype and implants-based oral rehabilitation in Ectodermal Dysplasia with WNT10A gene mutation: report of a case and literature reviewFrancois Clauss, Etienne Waltmann, Philippe Barriere, et al.
Journal of the American Academy of Dermatology|January 25, 2011
Clinical and histologic features of incontinentia pigmenti in adults with nuclear factor-κB essential modulator gene mutationsSmaïl Hadj-Rabia, Aude Rimella, Asma Smahi, et al.
Archives of Dermatology|September 17, 2003
Clinical study of 40 cases of incontinentia pigmentiSmaïl Hadj-Rabia, David Froidevaux, Nathalie Bodak, et al.
The Journal of Investigative Dermatology|January 28, 2006
Three severe cases of EBS Dowling-Meara caused by missense and frameshift mutations in the keratin 14 geneMatthias Titeux, Juliette Mazereeuw-Hautier, Smaïl Hadj-Rabia, et al.
Archives of Dermatology|September 24, 2004
Skin markers of occult spinal dysraphism in children: a review of 54 casesDavid Guggisberg, Smaïl Hadj-Rabia, Caroline Viney, et al.
Investigative Ophthalmology & Visual Science|February 14, 2025
Chiasmal Decussation in Oculo-Cutaneous Albinism Type 8Maxence Rateaux, Smaïl Hadj-Rabia, Rémi Barrois, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Dermatology (Basel, Switzerland)|August 22, 2012
Tibial lymphoplasmacytic plaque: a new, illustrative case of a recently and poorly recognized benign lesion in childrenIsabelle Moulonguet, Smaïl Hadj-Rabia, Nicolas Gounod, et al.
Pediatric Dermatology|January 4, 2012
Congenital erosive and vesicular dermatosis: a new case and review of the literatureJacob Mashiah, Daniel Wallach, Stéphanie Leclerc-Mercier, et al.
European Journal of Human Genetics : EJHG|August 27, 2003
The Rapp-Hodgkin syndrome results from mutations of the TP63 geneGaëlle Bougeard, Smaïl Hadj-Rabia, Laurence Faivre, et al.
International Journal of Molecular Sciences|July 9, 2022
The Fate of Epidermal Tight Junctions in the <i>stratum corneum</i>: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin ConditionsMarek Haftek, Vinzenz Oji, Laurence Feldmeyer, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|April 8, 2014
Dento-maxillo-facial phenotype and implants-based oral rehabilitation in Ectodermal Dysplasia with WNT10A gene mutation: report of a case and literature reviewFrancois Clauss, Etienne Waltmann, Philippe Barriere, et al.
Journal of the American Academy of Dermatology|January 25, 2011
Clinical and histologic features of incontinentia pigmenti in adults with nuclear factor-κB essential modulator gene mutationsSmaïl Hadj-Rabia, Aude Rimella, Asma Smahi, et al.
Archives of Dermatology|September 17, 2003
Clinical study of 40 cases of incontinentia pigmentiSmaïl Hadj-Rabia, David Froidevaux, Nathalie Bodak, et al.
The Journal of Investigative Dermatology|January 28, 2006
Three severe cases of EBS Dowling-Meara caused by missense and frameshift mutations in the keratin 14 geneMatthias Titeux, Juliette Mazereeuw-Hautier, Smaïl Hadj-Rabia, et al.
Archives of Dermatology|September 24, 2004
Skin markers of occult spinal dysraphism in children: a review of 54 casesDavid Guggisberg, Smaïl Hadj-Rabia, Caroline Viney, et al.
Investigative Ophthalmology & Visual Science|February 14, 2025
Chiasmal Decussation in Oculo-Cutaneous Albinism Type 8Maxence Rateaux, Smaïl Hadj-Rabia, Rémi Barrois, et al.
Pageof 3